Canonical Allele Identifier: CA349399015

Gene: PRKRA CHROMR

Linked Data

• COSMIC: COSM3570336
• MyVariant Identifiers: chr2:g.179296927G>A (hg19) ; chr2:g.178432200G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178432200G>A , CM000664.2:g.178432200G>A	GRCh38
NC_000002.11:g.179296927G>A , CM000664.1:g.179296927G>A	GRCh37
NC_000002.10:g.179005173G>A	NCBI36
NG_009053.1:g.24032C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000325748.9:c.839C>T (PRKRA) MANE Select	ENSP00000318176.4:p.Pro280Leu
ENST00000448279.2:c.*567C>T (PRKRA)	ENSP00000388455.1:n.*567C>T
ENST00000457633.2:c.*343C>T (PRKRA)	ENSP00000408668.2:n.*343C>T
ENST00000474793.6:n.980C>T (PRKRA)
ENST00000676505.1:c.*599C>T (PRKRA)	ENSP00000504163.1:n.*599C>T
ENST00000676586.1:n.2976C>T (PRKRA)
ENST00000676752.1:n.2738C>T (PRKRA)
ENST00000676832.1:c.*660C>T (PRKRA)	ENSP00000503231.1:n.*660C>T
ENST00000676922.1:c.*567C>T (PRKRA)	ENSP00000503369.1:n.*567C>T
ENST00000677136.1:n.2831C>T (PRKRA)
ENST00000677206.1:c.*631C>T (PRKRA)	ENSP00000503034.1:n.*631C>T
ENST00000677253.1:c.*536C>T (PRKRA)	ENSP00000503466.1:n.*536C>T
ENST00000677386.1:c.*282C>T (PRKRA)	ENSP00000503003.1:n.*282C>T
ENST00000677460.1:c.*168C>T (PRKRA)	ENSP00000504507.1:n.*168C>T
ENST00000677584.1:c.*677C>T (PRKRA)	ENSP00000504411.1:n.*677C>T
ENST00000677689.1:c.584C>T (PRKRA)	ENSP00000502919.1:p.Pro195Leu
ENST00000677859.1:c.692C>T (PRKRA)
ENST00000677981.1:c.587C>T (PRKRA)	ENSP00000503536.1:p.Pro196Leu
ENST00000678053.1:c.*599C>T (PRKRA)	ENSP00000504330.1:n.*599C>T
ENST00000678058.1:c.583C>T (PRKRA)	ENSP00000503203.1:n.583C>T
ENST00000678167.1:c.*393C>T (PRKRA)	ENSP00000504479.1:n.*393C>T
ENST00000678775.1:c.500C>T (PRKRA)	ENSP00000504030.1:p.Pro167Leu
ENST00000678845.1:c.500C>T (PRKRA)	ENSP00000503011.1:p.Pro167Leu
ENST00000679037.1:c.*507C>T (PRKRA)	ENSP00000504421.1:n.*507C>T
ENST00000679202.1:n.1926C>T (PRKRA)
ENST00000325748.8:c.839C>T (PRKRA)	ENSP00000318176.4:p.Pro280Leu
ENST00000424699.5:c.*631C>T (PRKRA)	ENSP00000408029.1:n.*631C>T
ENST00000432031.6:c.806C>T (PRKRA)	ENSP00000393883.2:p.Pro269Leu
ENST00000487082.5:c.764C>T (PRKRA)	ENSP00000430604.1:p.Pro255Leu
ENST00000490501.5:n.1066C>T (PRKRA)
NM_001139517.1:c.806C>T (PRKRA)	NP_001132989.1:p.Pro269Leu
NM_001139518.1:c.764C>T (PRKRA)	NP_001132990.1:p.Pro255Leu
NM_001316362.1:c.500C>T (PRKRA)	NP_001303291.1:p.Pro167Leu
NM_003690.4:c.839C>T (PRKRA)	NP_003681.1:p.Pro280Leu
NR_110204.1:n.872-1182G>A (CHROMR)
NR_110205.1:n.716-1182G>A (CHROMR)
NR_110206.1:n.651-1182G>A (CHROMR)
XM_005246921.3:c.500C>T (PRKRA)	XP_005246978.1:p.Pro167Leu
XM_011512063.1:c.584C>T (PRKRA)	XP_011510365.1:p.Pro195Leu
XM_011512064.1:c.584C>T (PRKRA)	XP_011510366.1:p.Pro195Leu
XM_011512066.1:c.500C>T (PRKRA)	XP_011510368.1:p.Pro167Leu
XM_011512063.2:c.584C>T (PRKRA)	XP_011510365.1:p.Pro195Leu
XM_011512066.2:c.500C>T (PRKRA)	XP_011510368.1:p.Pro167Leu
XM_017005159.1:c.500C>T (PRKRA)	XP_016860648.1:p.Pro167Leu
XR_001739008.2:n.880C>T (PRKRA)
NM_003690.5:c.839C>T (PRKRA) MANE Select	NP_003681.1:p.Pro280Leu
NM_001316362.2:c.500C>T (PRKRA)	NP_001303291.1:p.Pro167Leu